Positive electrode active material for non-aqueous electrolyte secondary cell and cell using the same

a technology active materials, which is applied in the direction of cell components, conductors, and nickel compounds, can solve the problems of non-aqueous electrolyte secondary batteries, high electromotive force and high energy density, and decrease in discharge capacity during charge/discharge cycles, so as to suppress the effect of battery thickness increas

Inactive Publication Date: 2006-01-31
PANASONIC CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0008]The present invention solves the foregoing problems and it has an object of improving a positive electrode active material to suppress an increase in battery thickness due to repeated charge / discharge cycles, thereby retaining the discharge capacity and thermal stability of a battery.

Problems solved by technology

Non-aqueous electrolyte secondary batteries, which have been recently used in various fields, have high electromotive force and high energy density.
In such an occasion, the positive electrode active material undergoes distortion, structural destruction and pulverization, resulting in a problem of a decrease in the discharge capacity during charge / discharge cycles.
In the case of square batteries or laminated batteries, the problem of an increase in battery thickness needs to be addressed because the cases thereof have poor strength.
However, also in this case, the battery thickness gradually increases owing to repeated charge / discharge cycles.
It is considered that repeated charge / discharge cycles increase distortion between these layers, resulting in an expansion of the crystal lattice.
As described above, since conventional positive electrode active materials undergo distortion, structural destruction and pulverization due to repeated charge / discharge cycles, they have a disadvantage of increasing the battery thickness and decreasing the discharge capacity.
As a result, although the batteries have high thermal stability during the initial charge / discharge period, they have another disadvantage that the structure of the positive electrode active materials become unstable to cause an insufficient thermal stability after repeated charge / discharge cycles.

Method used

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  • Positive electrode active material for non-aqueous electrolyte secondary cell and cell using the same

Examples

Experimental program
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example 1

(i) Fabrication of Positive Electrode

[0058]A positive electrode active material having the composition formula (Li0.95Al0.05)(Co0.9Al0.1)O2 was synthesized in the following manner.

[0059]An aqueous solution containing cobalt sulfate at a concentration of 0.9 mol / l and aluminium sulfate at a concentration of 0.1 mol / l was prepared. While adding dropwise an aqueous solution of sodium hydroxide such that the pH of the above solution was 10 to 13, the respective materials were continuously supplied to a reaction vessel thereby to synthesize a precursor comprising a hydroxide (Co0.9Al0.1)(OH)2.

[0060]The obtained precursor, lithium carbonate and aluminium hydroxide were mixed such that the molar ratio of the total amount of cobalt and aluminium in the precursor, the amount of lithium in lithium carbonate and the amount of aluminium in aluminium hydroxide was 1:0.95:0.05. After temporarily baked at 600° C., the mixture was pulverized and subsequently baked again at 900° C., followed by pulv...

example 2

[0068]A precursor comprising a hydroxide (Co0.9Cu0.1)(OH)2 was synthesized in the same manner as in Example 1 except for the use of copper sulfate in place of aluminium sulfate.

[0069]Further, the precursor was used to produce a positive electrode active material (Li0.95Cu0.05)(Co0.9Cu0.1)O2 in the same manner as in Example 1 except for the use of copper carbonate in place of aluminium hydroxide, and this was used to fabricate Battery 2A similar to Battery 1A.

example 3

[0070]A precursor comprising a hydroxide (Co0.9Zn0.1)(OH)2 was synthesized in the same manner as in Example 1 except for the use of zinc sulfate in place of aluminium sulfate.

[0071]Further, the precursor was used to produce a positive electrode active material (Li0.95Zn0.5)(Co0.9Zn0.1)O2 in the same manner as in Example 1 except for the use of zinc oxide in place of aluminium hydroxide, and this was used to fabricate Battery 3A similar to Battery 1A.

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Abstract

There is provided a positive electrode active material for a non-aqueous electrolyte secondary battery, comprising a composite oxide represented by the general formula (1): (Li1-xMx)a(Co1-yMy)bOc where lithium and cobalt are partly replaced with element M in the crystal structure of LiCoOc, wherein element M is at least one selected from the group consisting of Al, Cu, Zn, Mg, Ca, Ba and Sr, and 0.02≦x+y≦0.15, 0.90≦a / b≦1.10, and 1.8≦c≦2.2 are satisfied.

Description

TECHNICAL FIELD[0001]The present invention relates to a positive electrode active material for a non-aqueous electrolyte secondary battery and a non-aqueous electrolyte secondary battery for use in, for example, personal digital assistants, portable electronic appliances and home-use power storage devices as well as two-wheeled motor vehicles, electric vehicles and hybrid electric vehicles, each of which employs a motor as the power source.BACKGROUND ART[0002]Non-aqueous electrolyte secondary batteries, which have been recently used in various fields, have high electromotive force and high energy density. As the positive electrode active material for non-aqueous electrolyte secondary batteries, lithium cobaltate (LiCoO2) is mainly used. This substance has a high oxidation-reduction potential of 4 V or higher with respect to lithium.[0003]The above positive electrode active material repeatedly expands and contracts during charge / discharge. In such an occasion, the positive electrode ...

Claims

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Application Information

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Patent Type & Authority Patents(United States)
IPC IPC(8): H01B1/02C01G51/00H01M10/05H01M4/525H01M10/052
CPCC01G51/00C01G51/42C01G53/42H01M4/525H01M10/0525C01G51/04Y02E60/122C01P2002/52C01P2002/54C01P2002/76C01P2004/61C01P2006/12C01P2006/40H01M4/131H01M4/133H01M4/485H01M10/0587H01M2004/021Y02E60/10H01M4/48
Inventor NAGAYAMA, MASATOSHIYOSHIZAWA, HIROSHIARIMOTO, SHINJI
Owner PANASONIC CORP
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